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I2800

Sigma-Aldrich

Indene

contains 50-100 ppm tert-butylcatechol as stabilizer, technical grade, ≥90%

Synonym(s):

Indonaphthene

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About This Item

Empirical Formula (Hill Notation):
C9H8
CAS Number:
95-13-6
Molecular Weight:
116.16
Beilstein:
635873
EC Number:
202-393-6
MDL number:
MFCD00003777
UNSPSC Code:
12352100
PubChem Substance ID:
24896009
NACRES:
NA.22

grade

technical grade

Quality Level

100

Assay

≥90%

form

liquid

contains

50-100 ppm tert-butylcatechol as stabilizer

refractive index

n20/D 1.595 (lit.)

bp

181-182 °C (lit.)

mp

−5-−3 °C (lit.)

density

0.996 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

C1C=Cc2ccccc12

InChI

1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2

InChI key

YBYIRNPNPLQARY-UHFFFAOYSA-N

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Related Categories

Pictograms

FlameHealth hazard
GHS02,GHS08

Signal Word

Danger

Hazard Statements

H226,H304

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

136.4 °F - closed cup

Flash Point(C)

58 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

I2800-BULK:
I2800-5ML:
I2800-1L:4548173949796
I2800-250G:
I2800-25KG:
I2800-VAR:
I2800-1KG:
I2800-250ML:4548173949802
I2800-5KG:
I2800-10KG:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Helga Seyler et al.
The Journal of organic chemistry, 76(9), 3551-3556 (2011-03-12)
Various fullerene-based electron acceptor materials for organic photovoltaic applications were prepared via [3+2] and [4+2] cycloadditions using a continuous flow approach. The 1,3-dipolar cycloaddition of the tosylhydrazone precursor and the Diels-Alder cycloaddition of indene to either C(60) or C(70) under
Ermitas Alcalde et al.
Journal of medicinal chemistry, 52(3), 675-687 (2009-01-23)
Scaffold selection involving an indole-to-indene core change led to the discovery of a series of indenylsulfonamides that act as 5-HT6 serotonin receptor agonists. The variety of the targeted ligands and their synthetic complexity required multistep synthetic approaches. The novel indenylsulfonamides
Ram Shankar Upadhayaya et al.
Organic & biomolecular chemistry, 8(24), 5661-5673 (2010-10-12)
Prompted by our discovery of a new class of conformationally-locked indeno[2,1-c]quinolines as anti-mycobacterials, compounds 2a and 3a (Fig. 1; MIC < 0.39 μg mL(-1) and 0.78 μg mL(-1), respectively)(14) with a freely rotating C2-imidazolo substituent, we herein describe the synthesis
Hiroaki Kurouchi et al.
Journal of the American Chemical Society, 132(2), 807-815 (2009-12-19)
The chemical features, such as substrate stability, product distribution, and substrate generality, and the reaction mechanism of Brønsted superacid-catalyzed cyclization reactions of aromatic ring-containing acetoacetates (beta-ketoesters) were examined in detail. While two types of carbonyl cyclization are possible, i.e., keto
Lucas J Gursky et al.
Applied microbiology and biotechnology, 85(4), 995-1004 (2009-07-02)
The styAB genes from Pseudomonas putida CA-3, which encode styrene monooxygenase, were subjected to three rounds of in vitro evolution using error-prone polymerase chain reaction with a view to improving the rate of styrene oxide and indene oxide formation. Improvements
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